New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy

New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy

Introduction: Arrhythmogenic cardiomyopathy (ACM) is an inherited disease characterized by progressive fibroadipose replacement of cardiomyocytes. Its diagnosis is based on imaging, electrocardiographic, histological and genetic/familial criteria. The development of the disease is based mainly on de...

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Bibliographic Details
Main Authors: Fiama Caimi-Martinez, Guido Antoniutti, Rocio Blanco, Bernardo García de la Villa, Nelson Alvarenga, Nancy Govea-Callizo, Laura Torres-Juan, Damián Heine-Suñer, Jordi Rosell-Andreo, David Crémer Luengos, Jorge Alvarez-Rubio, Tomás Ripoll-Vera
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Genes
Subjects:
cardiomyopathies
CVD genetics
NGS for diagnostics of CVDs-
Online Access:https://www.mdpi.com/2073-4425/13/5/782

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https://www.mdpi.com/2073-4425/13/5/782

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